The CRA is as such responsible for recruitment at site level. The CRA thereby delivers results that have a direct impact on the successful completion of the clinical programme.
Candidate should have exposure in analysis of Content Uniformity, Blend Uniformity, Hold Time Study, Cleaning Validation Test and Finish Product Analysis.
Exposure of analysis for Finished Products, Stability Samples & Raw Materials. Having Knowledge of Analytical Method Validation, Verification & Method Transfer. Having skill for data interpretation, troubleshooting. Pharma knowledge of Solid orals & Quality process.
To perform all associate activities like reagent preparation, volumetric solution preparation, test solution preparation, factor determination, working standard preparation required for analysis as per approved procedure.
Candidate should have Exposure of Fette, Sejong, Legacy, Korsch, Cadmach or any other machine having Automatic Weight Control , Compaction Force Control etc.
Teva is on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day.